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Cognitive and behavioral profile of Perry syndrome in two families.

Parkinsonism & related disorders - 1 Aug 2020

Milanowski Łukasz, Sitek Emilia J, Dulski Jarosław, Cerquera-Cleves Catalina, Gomez Juan D, Brockhuis Bogna, Schinwelski Michał, Kluj-Kozłowska Klaudia, Ross Owen A, Sławek Jarosław, Wszolek Zbigniew K

Abstract excerpt

OBJECTIVE: Perry syndrome (PS) is a rare neurodegenerative disorder with autosomal dominant inheritance caused by point mutations in DCTN1 and characterized by parkinsonism, hypoventilation, weight loss, and psychiatric symptoms. Even though behavioral manifestation is a main feature of PS, detailed neuropsychological assessment was not performed in this cohort. In this study, the neuropsychological profile of...

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PMID: 32717578
DOI: 10.1016/j.parkreldis.2020.05.019

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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